A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615275



Internal ID16402684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123346788..123348027hg38UCSC Ensembl
Innerchr9:126109067..126110306hg19UCSC Ensembl
Innerchr9:125148888..125150127hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg381240
hg191240
hg181240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12863n54
Supporting Variantsnssv1141300, nssv1141302, nssv1141301
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615275
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer